NDC 0115-6811 – Bupropion Hydrochloride

Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC0115-6811

Product details

Brand name
Bupropion Hydrochloride
Generic name
Bupropion Hydrochloride
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA077415
Marketed since
May 1, 2009
Listing expires
December 31, 2026
Pharmacologic class
Aminoketone

Active ingredients

Uses, dosage, side effects and warnings for Bupropion hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
0115-6811-02500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6811-02)May 1, 2009
0115-6811-0830 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6811-08)May 1, 2009
0115-6811-1090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6811-10)May 1, 2009

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